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首页> 外文期刊>Arabian journal of chemistry >Synthesis, in vitro antimicrobial, anticancer evaluation and QSAR studies of N'-(substituted)-4-(butan-2-lideneamino)benzohydrazides
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Synthesis, in vitro antimicrobial, anticancer evaluation and QSAR studies of N'-(substituted)-4-(butan-2-lideneamino)benzohydrazides

机译:N'-(取代)-4-(丁二-2-亚氨基氨基)苯甲酰肼的合成,体外抗菌,抗癌评估和QSAR研究

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摘要

A series of N-(substituted)-4-(butan-2-ylideneamino)benzohydrazides (1-21) was synthesized and characterized by physicochemical as well as spectral means. The synthesized compounds were screened for their in vitro antimicrobial and anticancer potentials. The synthesized compounds displayed higher antifungal potential as compared to antibacterial potential. Besided having good antifungal potential, the synthesized compounds were having appreciable anticancer potential and a number of compounds displayed higher anticancer potential than the standard drug, carboplatin. The results of QSAR studies demonstrated the importance of steric parameter molar refractivity (MR), topological parameters, third order molecular connectivity index (~3x) Kier's first order shape index (k1) in describing the antimicrobial activity of N'-(substituted)-4-(butan-2-ylideneamino)benzohydrazides.
机译:合成了一系列N-(取代)-4-(丁-2-亚氨基氨基)苯并酰肼(1-21),并通过理化和光谱手段对其进行了表征。筛选合成的化合物的体外抗菌和抗癌潜力。与抗菌潜力相比,合成的化合物显示出更高的抗真菌潜力。除了具有良好的抗真菌潜力外,合成的化合物还具有明显的抗癌潜力,并且许多化合物均比标准药物卡铂具有更高的抗癌潜力。 QSAR研究结果表明,空间参数摩尔折射率(MR),拓扑参数,三阶分子连接指数(〜3x)在描述N'-(取代)-的抗菌活性时,Kier的一阶形状指数(k1)十分重要。 4-(丁-2-亚烷基氨基)苯甲酰肼。

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